Kiryanova Veronika, Meunier Sara J, Dyck Richard H
Department of Psychology, University of Calgary, Calgary, Alberta, Canada; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Department of Psychology, University of Calgary, Calgary, Alberta, Canada; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Behav Brain Res. 2017 Jul 28;331:84-91. doi: 10.1016/j.bbr.2017.05.029. Epub 2017 May 13.
Depression, anxiety, and stress are common in pregnant women. One of the primary pharmacological treatments for anxiety and depression is the antidepressant fluoxetine (Flx). Maternal stress, depression, and Flx exposure are known to effect neurodevelopment of the offspring, however, their combined effects have been scarcely studied, especially in female offspring. The present study investigated the combined effects of maternal stress during pregnancy and perinatal exposure to Flx on the behaviour of female mice as adults.
Mouse dams were exposed to either chronic unpredictable stress (embryonic (E) day 7 to E18), or FLX (E15- postnatal day 12), or a combination of stress and FLX or left untreated. At two months of age, the female offspring went through a comprehensive behavioural test battery.
Maternal stress led to increased activity and alterations of prepulse inhibition in the adult female offspring. Maternal treatment with Flx had a potentially beneficial effect on spatial memory. The combination of prenatal stress and perinatal Flx exposure did not interact in their effects. These results suggest that gestational Flx exposure may have a limited negative impact on female offspring.
抑郁、焦虑和压力在孕妇中很常见。抗抑郁药氟西汀(Flx)是治疗焦虑和抑郁的主要药物之一。已知母体压力、抑郁和接触氟西汀会影响后代的神经发育,然而,它们的综合影响很少被研究,尤其是对雌性后代。本研究调查了孕期母体压力和围产期接触氟西汀对成年雌性小鼠行为的综合影响。
将母鼠暴露于慢性不可预测应激(胚胎期(E)第7天至E18天)、氟西汀(E15至出生后第12天)、应激与氟西汀的组合或不进行处理。在两个月大时,雌性后代接受了全面的行为测试。
母体压力导致成年雌性后代活动增加和前脉冲抑制改变。用氟西汀对母体进行治疗对空间记忆有潜在的有益影响。产前应激和围产期接触氟西汀的组合在其影响方面没有相互作用。这些结果表明,孕期接触氟西汀可能对雌性后代有有限的负面影响。